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C18<br />

Mechanisms of<br />

Separation<br />

Hydrophobic binding<br />

interactions<br />

Shape selectivity<br />

Target Analytes<br />

Analytes differing in hydrophobicity<br />

Polar, moderately polar and nonpolar analytes<br />

Uncharged acids and bases<br />

Ionized acids or bases using ion-pairing<br />

Recommended Applications<br />

Analytes differing in hydrophobicity<br />

Strength of<br />

Interaction<br />

Strong<br />

Weak<br />

Homologous compounds differing by –CH2<br />

Ideal starting point for method development<br />

Further Information;<br />

An HPLC product brochure discussing ACE C18 and all<br />

ACE phases is available.<br />

Contact your distributor to request your copy or visit<br />

www.ace-hplc.com for further details.<br />

6<br />

Figure 6: Comparison of selectivity and characteristics of<br />

ACE ® <strong>Excel</strong> TM<br />

2µm C18 to other manufacturers’ columns<br />

Application #1503 – Rapid UHPLC Screening of 16 Pharmaceuticals and Related Compounds<br />

Mobile Phase: A = 20 mM KH 2 PO 4 , pH 2.7 and<br />

B = 20 mM KH 2 PO 4 , pH 2.7 in MeOH/H 2 O (65:35 v/v)<br />

Gradient: 3 to 100% B in 5 minutes<br />

Flow Rate: 0.6 ml/min<br />

Temperature: 60°C<br />

Detection: UV, 214 nm<br />

Column Dimensions: 50 x 2.1mm<br />

ACE <strong>Excel</strong> 2 C18<br />

ZORBAX Eclipse<br />

1.8 XDB C18<br />

Waters ACQUITY<br />

1.7 BEH C18<br />

Phenomenex<br />

Kinetex 1.7 C18<br />

0<br />

1<br />

2<br />

1<br />

1,2<br />

1<br />

1. N-acetylprocainamide<br />

2. 3-hydroxybenzoic acid<br />

3. pindolol<br />

4. methylphenylsulphoxide<br />

5. benzylalcohol<br />

6. quinoxaline<br />

7. 1,4-dinitrobenzene<br />

8. phenacetin<br />

Comparative data may not be representative of all applications.<br />

Please see p.10 for acknowledgement of trademarks<br />

2<br />

1<br />

3,4<br />

2<br />

3<br />

4<br />

5<br />

3<br />

5<br />

3<br />

4<br />

5<br />

4<br />

5<br />

6<br />

2<br />

6<br />

7<br />

6<br />

6<br />

7<br />

Minutes<br />

9. 1,2-dimethoxybenzene<br />

10. furosemide<br />

11. anisole<br />

12. methylbenzoate<br />

13. remacemide<br />

14. nimesulide<br />

15. ethylbenzoate<br />

16. diflunisal<br />

In this example the ACE <strong>Excel</strong> C18 UHPLC column provides retention<br />

and selectivity similar to the other C18 UHPLC columns (although<br />

there may be slight selectivity differences between different C18<br />

phases). Under these conditions, these slight differences allow the ACE<br />

<strong>Excel</strong> C18 to fully separate all 16 components of interest.<br />

As with all ACE HPLC columns, ACE <strong>Excel</strong> UHPLC columns also deliver<br />

excellent peak shape for your analytes. Additionally, owing to the<br />

optimal 2µm particle size and a rigorous classification protocol, back<br />

pressure for all ACE <strong>Excel</strong> UHPLC columns is significantly lower than<br />

for these leading UHPLC columns packed with

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